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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
7
|
| pubmed:dateCreated |
1998-11-6
|
| pubmed:abstractText |
Two affected siblings with infantile spinal muscular atrophy (SMA I) presented with generalized muscular hypotonia, which progressed to early death. Quadriceps muscle biopsy did not show the typical neurogenic pattern of spinal muscular atrophy. The histochemical fiber type determination revealed a predominance of type II fibers without type I hypertrophy, an unprecedented finding in spinal muscular atrophy. Sural nerve biopsy exhibited findings typical for axonal neuropathy. In one patient, electrical stimulation of peripheral nerves showed an inexcitability of motor and sensory nerves. Genetic studies revealed homozygous deletions of the telomeric survival motor neuron (SMN) gene and the neuronal apoptosis inhibitory protein (NAIP) gene in the affected children. This is the second case report of molecular genetically proven spinal muscular atrophy associated with axonal neuropathy. We conclude atypical findings on muscle biopsy and evidence of axonal neuropathy are compatible with the diagnosis of infantile spinal muscular atrophy.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0883-0738
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
13
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
327-31
|
| pubmed:dateRevised |
2008-5-14
|
| pubmed:meshHeading |
pubmed-meshheading:9701481-Adult,
pubmed-meshheading:9701481-Apoptosis,
pubmed-meshheading:9701481-Axons,
pubmed-meshheading:9701481-Biopsy,
pubmed-meshheading:9701481-Chromosome Deletion,
pubmed-meshheading:9701481-Female,
pubmed-meshheading:9701481-Homozygote,
pubmed-meshheading:9701481-Humans,
pubmed-meshheading:9701481-Infant,
pubmed-meshheading:9701481-Infant, Newborn,
pubmed-meshheading:9701481-Male,
pubmed-meshheading:9701481-Motor Neurons,
pubmed-meshheading:9701481-Myofibrils,
pubmed-meshheading:9701481-Nerve Tissue Proteins,
pubmed-meshheading:9701481-Neuronal Apoptosis-Inhibitory Protein,
pubmed-meshheading:9701481-Pedigree,
pubmed-meshheading:9701481-Pregnancy,
pubmed-meshheading:9701481-Spinal Muscular Atrophies of Childhood,
pubmed-meshheading:9701481-Sural Nerve
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
|
| pubmed:affiliation |
Department of Neuropediatrics and Muscular Diseases, Albert-Ludwigs-Universität, Freiburg, Germany.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|